Canonical Allele Identifier: CA794017949
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1471454760
gnomAD v3: 4-3256738-TG-T
gnomAD v4: 4-3256738-TG-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256739del , CM000666.2:g.3256739del GRCh38
NC_000004.11:g.3258466del , CM000666.1:g.3258466del GRCh37
NC_000004.10:g.3228264del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+882del ENSP00000425405.1:n.729+882del
ENST00000510580.1:c.765+846del ENSP00000420966.1:n.765+846del
XM_011513464.1:c.729+882del XP_011511766.1:n.729+882del
XR_924950.1:n.753+882del